全文获取类型
收费全文 | 4032篇 |
免费 | 281篇 |
国内免费 | 3篇 |
出版年
2023年 | 21篇 |
2022年 | 40篇 |
2021年 | 74篇 |
2020年 | 58篇 |
2019年 | 64篇 |
2018年 | 89篇 |
2017年 | 76篇 |
2016年 | 135篇 |
2015年 | 222篇 |
2014年 | 230篇 |
2013年 | 271篇 |
2012年 | 341篇 |
2011年 | 325篇 |
2010年 | 182篇 |
2009年 | 179篇 |
2008年 | 251篇 |
2007年 | 232篇 |
2006年 | 183篇 |
2005年 | 180篇 |
2004年 | 189篇 |
2003年 | 173篇 |
2002年 | 115篇 |
2001年 | 75篇 |
2000年 | 80篇 |
1999年 | 74篇 |
1998年 | 22篇 |
1997年 | 25篇 |
1996年 | 26篇 |
1995年 | 18篇 |
1994年 | 10篇 |
1993年 | 14篇 |
1992年 | 29篇 |
1991年 | 21篇 |
1990年 | 18篇 |
1989年 | 15篇 |
1988年 | 19篇 |
1987年 | 18篇 |
1986年 | 21篇 |
1985年 | 16篇 |
1984年 | 14篇 |
1983年 | 13篇 |
1982年 | 11篇 |
1981年 | 13篇 |
1980年 | 13篇 |
1979年 | 14篇 |
1977年 | 8篇 |
1975年 | 12篇 |
1974年 | 11篇 |
1972年 | 8篇 |
1971年 | 7篇 |
排序方式: 共有4316条查询结果,搜索用时 31 毫秒
71.
Han K Lee JE Kwon SJ Park SY Shim SH Kim H Moon JH Suh CS Lim HJ 《Cell proliferation》2008,41(5):709-725
Abstract. Objectives: Human amnion is an easy‐to‐obtain novel source of human mesenchymal stem cells, which poses little or no ethical dilemmas. We have previously shown that human amnion‐derived mesenchymal (HAM) cells exhibit certain mesenchymal stem cell‐like characteristics with respect to expression of stem cell markers and differentiation potentials. Materials and methods: In this study, we further characterized HAM cells’ potential for in vivo therapeutic application. Results: Flow cytometric analyses of HAM cells show that they express several stem cell‐related cell surface markers, including CD90, CD105, CD59, CD49d, CD44 and HLA‐ABC, but not CD45, CD34, CD31, CD106 or HLA‐DR. HAM cells at the 10th passage showed normal karyotype. More interestingly, the AbdB‐like HOXA genes HOXA9, HOXA10 and HOXA11 that are expressed in the mesenchyme of the developing female reproductive tract and pregnant uteri are also expressed in HAM cells, suggesting similarities between these two mesenchymal cell types. Progesterone receptor is also highly expressed in HAM cells and expression of genes or proteins in HAM cells could be manipulated with the aid of lentivirus technology or cell‐permeable peptides. To test potentials of HAM cells for in vivo application, we introduced enhanced green fluorescence protein (EGFP)‐expressing HAM cells to mice by intrauterine infusion (into uteri) or by intravenous injection (into the circulation). Presence of EGFP‐expressing cells within the uterine mesenchyme after intrauterine infusion or in lungs after intravenous injection was noted within 1–4 weeks. Conclusions: Collectively, these results suggest that HAM cells are a potential source of mesenchymal stem cells with therapeutic potential. 相似文献
72.
Ho Nam Chang Nag-Jong Kim Jongwon Kang Chang Moon Jeong 《Biotechnology and Bioprocess Engineering》2010,15(1):1-10
The typical biorefinery platforms are sugar, thermochemical (syngas), carbon-rich chains, and biogas platforms, each offering
unique advantages and disadvantages. The sugar platform uses hexose and pentose sugars extracted or converted from plant body
mass. The thermochemical (syngas) platform entails a chemical or biological conversion process using pyrolysis or gasification
of plants to produce biofuels. The carbon-rich chains platform is used to produce biodiesel from long-chain fatty acids or
glycerides. In the present work, we suggest a new platform using volatile fatty acids (VFAs) for the production of biofuels
and biochemicals production. The VFAs are short-chain fatty acids composed mainly of acetate and butyrate in the anaerobic
digestion (AD) process, which does not need sterilization, additional hydrolysis enzymes (cellulose or xylanase), or a high
cost pretreatment step. VFAs are easily produced from almost all kinds of biomass with low lignin content (terrestrial, aquatic,
and marine biomass) by the AD process. Considering that raw material alone constitutes 40∼80% of biofuel production costs,
biofuels made from VFAs derived from waste organic biomass potentially offer significant economical advantage. 相似文献
73.
Moon MW Park SY Choi SK Lee JK 《Journal of molecular microbiology and biotechnology》2007,12(1-2):43-50
In this review, we describe the phosphotransferase system (PTS) of Corynebacterium glutamicum and discuss genes for putative global carbon regulation associated with the PTS. C. glutamicum ATCC 13032 has PTS genes encoding the general phosphotransferases enzyme I, HPr and four enzyme II permeases, specific for glucose, fructose, sucrose and one yet unknown substrate. C. gluamicum has a peculiar sugar transport system involving fructose efflux after hydrolyzing sucrose transported via sucrose EII. Also, in addition to their primary PTS, fructose and glucose are each transported by a second transporter, glucose EII and a non-PTS permease, respectively. Interestingly, C. glutamicum does not show any preference for glucose, and thus co-metabolizes glucose with other sugars or organic acids. Studies on PTS-mediated sugar uptake and its related regulation in C. glutamicum are important because the production yield of lysine and cell growth are dependent on the PTS sugars used as substrates for fermentation. In many bacteria, the PTS is also involved in several regulatory processes. However, the detailed molecular mechanism of global carbon regulation associated with the PTS in this organism has not yet been revealed. 相似文献
74.
Cho KJ Shim JH Cho MC Choe YK Hong JT Moon DC Kim JW Yoon DY 《Journal of cellular biochemistry》2005,96(4):869-878
Melanocortins, besides their central roles, have also recently been reported to regulate adipocyte metabolism. In this study, we attempted to characterize the mechanism underlying alpha-melanocyte-stimulating hormone (MSH)-induced lipolysis, and compared it with that of the adrenocorticotrophin hormone (ACTH) in 3T3-L1 adipocytes. Similar to ACTH, MSH treatment resulted in the release of glycerol into the cell supernatant. The activity of hormone-sensitive lipase, a rate-limiting enzyme, which is involved in lipolysis, was significantly increased by MSH treatment. In addition, a variety of kinases, including protein kinase A (PKA) and extracellular signal-regulated kinase (ERK) were also phosphorylated as the result of MSH treatment, and their specific inhibitors caused a reduction in MSH-induced glycerol release and HSL activity, indicating that MSH-induced lipolysis was mediated by these kinases. These results suggest that PKA and ERK constitute the principal signaling pathways implicated in the MSH-induced lipolytic process via the regulation of HSL in 3T3-L1 adipocytes. 相似文献
75.
76.
Yu‐Sin Jang Alok Malaviya Joungmin Lee Jung Ae Im Sang Yup Lee Julia Lee Moon‐Ho Eom Jung‐Hee Cho Do Young Seung 《Biotechnology progress》2013,29(4):1083-1088
Butanol is considered as a superior biofuel, which is conventionally produced by clostridial acetone‐butanol‐ethanol (ABE) fermentation. Among ABE, only butanol and ethanol can be used as fuel alternatives. Coproduction of acetone thus causes lower yield of fuel alcohols. Thus, this study aimed at developing an improved Clostridium acetobutylicum strain possessing enhanced fuel alcohol production capability. For this, we previously developed a hyper ABE producing BKM19 strain was further engineered to convert acetone into isopropanol. The BKM19 strain was transformed with the plasmid pIPA100 containing the sadh (primary/secondary alcohol dehydrogenase) and hydG (putative electron transfer protein) genes from the Clostridium beijerinckii NRRL B593 cloned under the control of the thiolase promoter. The resulting BKM19 (pIPA100) strain produced 27.9 g/l isopropanol‐butanol‐ethanol (IBE) as a fuel alcohols with negligible amount of acetone (0.4 g/l) from 97.8 g/l glucose in lab‐scale (2 l) batch fermentation. Thus, this metabolically engineered strain was able to produce 99% of total solvent produced as fuel alcohols. The scalability and stability of BKM19 (pIPA100) were evaluated at 200 l pilot‐scale fermentation, which showed that the fuel alcohol yield could be improved to 0.37 g/g as compared to 0.29 g/g obtained at lab‐scale fermentation, while attaining a similar titer. To the best of our knowledge, this is the highest titer of IBE achieved and the first report on the large scale fermentation of C. acetobutylicum for IBE production. © 2013 American Institute of Chemical Engineers Biotechnol. Prog., 29:1083–1088, 2013 相似文献
77.
Il-Chan Kim Young Ja Kim Young-Mi Lee Bok-Geon Kim Tae-Jin Park Hyeung-Sin Kim Min-Min Jung Tim D Williams Wonchoel Lee Jae-Seong Lee 《DNA sequence》2004,15(2):159-163
We synthesized a cDNA library from the intertidal copepod Tigriopus japonicus, converted it to phagemids and sequenced expressed sequence tags (ESTs). Of these, Tigriopus translationally controlled tumor protein/histamine releasing factor (TCTP/HRF) was further characterized. The Tigriopus TCTP/HRF gene encoded 172 amino acid residues and showed high similarity to Drosophila but moderate similarity to other annelids (e.g. Brugia, Wuchereria and C. elegans). The Tigriopus TCTP/HRF gene appeared in the same clade as the annelids. Here, we describe the analysis of the Tigriopus TCTP/HRF gene. 相似文献
78.
79.
Development of monoclonal antibodies that identify Vibrio species commonly isolated from infections of humans, fish, and shellfish. 总被引:1,自引:3,他引:1
下载免费PDF全文
![点击此处可从《Applied microbiology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Monoclonal antibodies (MAbs) against Vibrio species that infect humans, fish, and shellfish were developed for application in rapid identifications. The pathogens included Vibrio alginolyticus, V. anguillarum, V. carchariae, V. cholerae, V. damsela, V. furnissii, V. harveyi, V. ordalii, V. parahaemolyticus, and V. vulnificus. Three types of MAbs were selected. The first important group included MAbs that reacted with only a single species. A second group comprised a number of MAbs that reacted with two, taxonomically closely related Vibrio species. For example, of 22 MAbs raised against V. alginolyticus, 6 recognized a 52-kDa flagellar H antigen common to both V. alginolyticus and V. parahaemolyticus; V. anguillarum and V. ordalii also shared antigens. A third group included three genus-specific MAbs that reacted with almost all Vibrio species but did not react with other members of the family Vibrionaceae (e.g., members of the Aeromonas, Photobacterium, and Plesiomonas genera) or a wide range of gram-negative bacteria representing many genera. This last group indicated the possible existence of an antigenic determinant common to Vibrio species. Two of these three genus-specific MAbs reacted with heat-stable antigenic determinants of Vibrio species as well as lipopolysaccharide extracted from Vibrio species. The use of the MAbs in blind tests and diagnosis of clinical isolates indicated that three different types of bacteria, viz., live, formalin-fixed, and sodium azide-killed bacteria, were detected consistently. Overall, it was found that the genus-specific MAbs were very useful for rapidly identifying vibrios in the screening of acute infections, while the species-specific MAbs and others were useful for completing the diagnosis. 相似文献
80.